RS376923877 TNNT2

Health Risk Chr 1:201359637
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What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Cardiomyopathy
Dilated cardiomyopathy 1D
Hypertrophic cardiomyopathy 2
familial restrictive
3
Cardiovascular phenotype
TNNT2-related disorder
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Cardiomyopathy
Dilated cardiomyopathy 1D
Hypertrophic cardiomyopathy 2
familial restrictive
3
Cardiovascular phenotype
Other Variants in TNNT2
rs121964855 rs121964856 rs121964858 rs74315379 rs74315380 rs121964860 rs193922620 rs377474357 rs397516447 rs397516448
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